| Literature DB >> 29795756 |
Kevin J Filipski1, Matthew F Sammons1, Samit K Bhattacharya1, Jane Panteleev2, Janice A Brown2, Paula M Loria2, Markus Boehm1, Aaron C Smith2, Andre Shavnya2, Edward L Conn2, Kun Song1, Yan Weng1, Carie Facemire1, Harald Jüppner3, Valerie Clerin1.
Abstract
Sodium-phosphate cotransporter 2a, or NaPi2a (SLC34A1), is a solute-carrier (SLC) transporter located in the kidney proximal tubule that reabsorbs glomerular-filtered phosphate. Inhibition of NaPi2a may enhance urinary phosphate excretion and correct maladaptive mineral and hormonal derangements associated with increased cardiovascular risk in chronic kidney disease-mineral and bone disorder (CKD-MBD). To date, only nonselective NaPi inhibitors have been described. Herein, we detail the discovery of the first series of selective NaPi2a inhibitors, resulting from optimization of a high-throughput screening hit. The oral PK profile of inhibitor PF-06869206 (6f) in rodents allows for the exploration of the pharmacology of selective NaPi2a inhibition.Entities:
Year: 2018 PMID: 29795756 PMCID: PMC5949730 DOI: 10.1021/acsmedchemlett.8b00013
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345